Androgen Regulation of 5α-Reductase Isoenzymes in Prostate Cancer: Implications for Prostate Cancer Prevention
Author(s) -
Jin Li,
Zhiyong Ding,
Zhengxin Wang,
Jing-Fang Lu,
Sankar N. Maity,
Nora M. Navone,
Christopher J. Logothetis,
Gordon B. Mills,
Jeri Kim
Publication year - 2011
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0028840
Subject(s) - dihydrotestosterone , androgen receptor , prostate cancer , isozyme , androgen , testosterone (patch) , reductase , cancer research , biology , prostate , endocrinology , medicine , cancer , enzyme , biochemistry , hormone
The enzyme 5α-reductase, which converts testosterone to dihydrotestosterone (DHT), performs key functions in the androgen receptor (AR) signaling pathway. The three isoenzymes of 5α-reductase identified to date are encoded by different genes: SRD5A1 , SRD5A2 , and SRD5A3 . In this study, we investigated mechanisms underlying androgen regulation of 5α-reductase isoenzyme expression in human prostate cells. We found that androgen regulates the mRNA level of 5α-reductase isoenzymes in a cell type–specific manner, that such regulation occurs at the transcriptional level, and that AR is necessary for this regulation. In addition, our results suggest that AR is recruited to a negative androgen response element (nARE) on the promoter of SRD5A3 in vivo and directly binds to the nARE in vitro . The different expression levels of 5α-reductase isoenzymes may confer response or resistance to 5α-reductase inhibitors and thus may have importance in prostate cancer prevention.
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